| dada2-package | DADA2 package |
| addSpecies | Add species-level annotation to a taxonomic table. |
| assignSpecies | Taxonomic assignment to the species level by exact matching. |
| assignTaxonomy | Classifies sequences against reference training dataset. |
| c-method | Change concatenation to list construction. |
| c-method | Change concatenation to list construction. |
| collapseNoMismatch | Combine together sequences that are identical up to shifts and/or length. |
| dada | High resolution sample inference from amplicon data. |
| dada-class | The object class returned by 'dada' |
| derep-class | A class representing dereplicated sequences |
| derepFastq | Read in and dereplicate a fastq file. |
| errBalancedF | An empirical error matrix. |
| errBalancedR | An empirical error matrix. |
| errExtremeF | An empirical error matrix. |
| errExtremeR | An empirical error matrix. |
| errHmpF | An empirical error matrix. |
| errHmpR | An empirical error matrix. |
| fastqFilter | Filter and trim a fastq file. |
| fastqPairedFilter | Filters and trims paired forward and reverse fastq files. |
| filterAndTrim | Filter and trim fastq file(s). |
| getDadaOpt | Get DADA options |
| getErrors | Extract already computed error rates. |
| getSequences | Get vector of sequences from input object. |
| getUniques | Get the uniques-vector from the input object. |
| inflateErr | Inflates an error rate matrix by a specified factor, while accounting for saturation. |
| isBimera | Determine if input sequence is a bimera of putative parent sequences. |
| isBimeraDenovo | Identify bimeras from collections of unique sequences. |
| isBimeraDenovoTable | Identify bimeras in a sequence table. |
| isPhiX | Determine if input sequence(s) match the phiX genome. |
| isShiftDenovo | Identify sequences that are identical to a more abundant sequence up to an overall shift. |
| learnErrors | Learns the error rates from an input list, or vector, of file names or a list of 'derep-class' objects. |
| loessErrfun | Use a loess fit to estimate error rates from transition counts. |
| makeSequenceTable | Construct a sample-by-sequence observation matrix. |
| mergePairs | Merge denoised forward and reverse reads. |
| mergePairsByID | Merge forward and reverse reads after DADA denoising, even if reads were not originally ordered together. |
| mergeSequenceTables | Merge two or more sample-by-sequence observation matrices. |
| names<--method | Deactivate renaming of dada-class objects. |
| names<--method | Deactivate renaming of derep-class objects. |
| noqualErrfun | Estimate error rates for each type of transition while ignoring quality scores. |
| nwalign | Needleman-Wunsch alignment. |
| nwhamming | Hamming distance after Needlman-Wunsch alignment. |
| PacBioErrfun | Estimate error rates from transition counts in PacBio CCS data. |
| plotErrors | Plot observed and estimated error rates. |
| plotQualityProfile | Plot quality profile of a fastq file. |
| removeBimeraDenovo | Remove bimeras from collections of unique sequences. |
| seqComplexity | Determine if input sequence(s) are low complexity. |
| setDadaOpt | Set DADA options |
| show-method | method extensions to show for dada2 objects. |
| tperr1 | An empirical error matrix. |
| uniques-vector | The named integer vector format used to represent collections of unique DNA sequences. |
| uniquesToFasta | Write a uniques vector to a FASTA file |
| writeFasta-method | Writes a named character vector of DNA sequences to a fasta file. Values are the sequences, and names are used for the id lines. |